ENST00000299697.12:c.485A>C
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ENSP00000299697.9:p.Glu162Ala
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ENST00000417693.8:c.599A>C
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ENSP00000407469.5:p.Glu200Ala
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ENST00000451102.7:c.560A>C
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ENSP00000414334.4:p.Glu187Ala
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ENST00000527284.6:c.563-1711A>C
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ENST00000527800.6:c.362A>C
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ENSP00000433770.1:p.Glu121Ala
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ENST00000544898.6:c.653A>C
MANE Select
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ENSP00000440898.2:p.Glu218Ala
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ENST00000567357.6:c.*511A>C
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ENSP00000457959.2:n.*511A>C
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ENST00000569718.6:c.391A>C
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ENSP00000464313.2:p.Ser131Arg
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ENST00000620035.5:c.409A>C
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ENSP00000483833.2:p.Ser137Arg
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ENST00000676538.1:c.236A>C
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ENST00000676904.1:c.124A>C
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ENST00000677296.1:n.35A>C
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ENST00000677379.1:c.294A>C
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ENSP00000503672.1:n.294A>C
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ENST00000677420.1:c.362A>C
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ENSP00000504648.1:p.Glu121Ala
|
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ENST00000677555.1:c.362A>C
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ENSP00000503331.1:p.Glu121Ala
|
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ENST00000677715.1:c.362A>C
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ENSP00000502950.1:p.Glu121Ala
|
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ENST00000677753.1:n.35A>C
|
|
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ENST00000677961.1:n.65A>C
|
|
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ENST00000678015.1:c.362A>C
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ENSP00000502959.1:p.Glu121Ala
|
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ENST00000678190.1:c.35A>C
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ENSP00000503824.1:p.Glu12Ala
|
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ENST00000678282.1:n.35A>C
|
|
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ENST00000678297.1:c.362A>C
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ENSP00000503472.1:p.Glu121Ala
|
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ENST00000299697.11:c.653A>C
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ENSP00000299697.8:p.Glu218Ala
|
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ENST00000417693.7:c.725A>C
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ENSP00000407469.4:p.Glu242Ala
|
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ENST00000451102.6:c.779A>C
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ENSP00000414334.3:p.Glu260Ala
|
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ENST00000525974.5:c.362A>C
|
ENSP00000434594.1:p.Glu121Ala
|
|
ENST00000527284.5:c.560A>C
|
ENSP00000435312.1:p.Glu187Ala
|
|
ENST00000527800.5:c.362A>C
|
ENSP00000433770.1:p.Glu121Ala
|
|
ENST00000544898.5:c.653A>C
|
ENSP00000440898.2:p.Glu218Ala
|
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ENST00000545043.6:c.578A>C
|
ENSP00000438143.2:p.Glu193Ala
|
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ENST00000561527.5:n.212A>C
|
|
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ENST00000561728.1:c.102A>C
|
|
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ENST00000561905.2:c.7A>C
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ENST00000562552.5:n.469A>C
|
|
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ENST00000563099.5:n.180A>C
|
|
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ENST00000563369.6:c.362A>C
|
ENSP00000463560.1:p.Glu121Ala
|
|
ENST00000563478.5:c.362A>C
|
ENSP00000462341.1:p.Glu121Ala
|
|
ENST00000564792.1:n.308A>C
|
|
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ENST00000564917.5:c.704A>C
|
ENSP00000455187.1:p.Glu235Ala
|
|
ENST00000567357.5:c.*511A>C
|
ENSP00000457959.1:n.*511A>C
|
|
ENST00000569718.5:c.378A>C
|
|
|
ENST00000620035.4:c.599A>C
|
ENSP00000483833.1:p.Glu200Ala
|
|
NM_001172643.1:c.560A>C
|
NP_001166114.1:p.Glu187Ala
|
|
NM_001172644.1:c.578A>C
|
NP_001166115.1:p.Glu193Ala
|
|
NM_001172645.1:c.599A>C
|
NP_001166116.1:p.Glu200Ala
|
|
NM_001271934.1:c.506A>C
|
NP_001258863.1:p.Glu169Ala
|
|
NM_001271935.1:c.391A>C
|
NP_001258864.1:p.Ser131Arg
|
|
NM_001272050.1:c.362A>C
|
NP_001258979.1:p.Glu121Ala
|
|
NM_004614.4:c.653A>C
|
NP_004605.4:p.Glu218Ala
|
|
NR_073520.1:n.1932A>C
|
|
|
NM_001172644.2:c.578A>C
|
NP_001166115.1:p.Glu193Ala
|
|
NM_001271934.2:c.506A>C
|
NP_001258863.1:p.Glu169Ala
|
|
NM_001272050.2:c.362A>C
|
NP_001258979.1:p.Glu121Ala
|
|
NM_004614.5:c.653A>C
MANE Select
|
NP_004605.4:p.Glu218Ala
|
|
NR_073520.2:n.1642A>C
|
|
|
NM_001172645.2:c.599A>C
|
NP_001166116.1:p.Glu200Ala
|
|